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EFINGER® Artery Hemostasis Compression Devices - Indonesia BPOM Medical Device Registration

EFINGER® Artery Hemostasis Compression Devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504320246. The device is manufactured by SHENZHEN RISING MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GOLDEN GLOBE MEDICA.

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BPOM Registered
Risk Class Kelas Resiko : B
EFINGER® Artery Hemostasis Compression Devices
Analysis ID: AKL 20504320246

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GOLDEN GLOBE MEDICA

AR Address

Sarana Industri Terpadu PIK Unit E 2 No.25 Jl. Kamal Muara, Penjaringan - Jakarta Utara Telp : 021-56982721 Fax : 021-56982720

Registration Date

Oct 25, 2023

Expiry Date

Jul 01, 2026

Product Type

Surgical Cardiology Equipment

Vascular clamp.

Non Radiation Electromedics

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